Nicola Wright

A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40phox and selective defects in neutrophil NADPH oxidase activity

Juan D. Matute, Andrés A. Arias, Nicola Wright et al. · Blood · 2009 · 415 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders

Asbjørg Stray‐Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon et al. · Journal of Allergy and Clinical Immunology · 2016 · 280 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency

Svjetlana Lovric, Sara Gonçalves, Heon Yung Gee et al. · Journal of Clinical Investigation · 2017 · 208 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Changes in electrical activity of the brain with vigilance

A. Belyavin, Nicola Wright · Electroencephalography and Clinical Neurophysiology · 1987 · 160 citations

Nursing, Neurobiology, Neuroscience +11

The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions

Christopher C. Dvorak, Élie Haddad, Jennifer Heimall et al. · Journal of Allergy and Clinical Immunology · 2022 · 125 citations · Full text

Life Sciences, Hematology, Immunology +10